ReviewAmerican journal of human genetics1990
The fragile X: progress toward solving the puzzle.
Review in American journal of human genetics, 1990. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 1 of them a synthesis that pooled it.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
11 citing papers in PubMed, 1 synthesis or guideline pooled it.
- Guidelines for the diagnosis of fragile X syndrome. National Fragile X Foundation.Journal of medical genetics · 1993Guideline
- Oxytocin and vasopressin systems in genetic syndromes and neurodevelopmental disorders.Brain research · 2014Review
- Application of FTA sample collection and DNA purification system on the determination of CTG trinucleotide repeat size by PCR-based Southern blotting.Journal of clinical laboratory analysis · 1999Article
- The FRAXE Syndrome: is it time for routine screening?American journal of human genetics · 1996Article
- A study of FRAXE in mentally retarded individuals referred for fragile X syndrome (FRAXA) testing in the United Kingdom.American journal of human genetics · 1996Article
- Founder effect in a Belgian-Dutch fragile X population.Human genetics · 1993Article
- Origins of the fragile X syndrome mutation.Journal of medical genetics · 1993Article
- The fragile X syndrome: isolation of the FMR-1 gene and characterization of the fragile X mutation.Chromosoma · 1992Review
- Estimating the stability of the proposed imprinted state of the fragile-X mutation when transmitted by females.Human genetics · 1992Article
- Physical map of human Xq27-qter: localizing the region of the fragile X mutation.Proceedings of the National Academy of Sciences of the United States of America · 1991Article
- Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
1 author.
Funding
No grant is acknowledged in the PubMed record.
Abstract
PubMed holds no abstract for this paper.
Indexed as
Identifiers
1974122PMC1683734What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.